Cargando…
Juvenile Hyaline Fibromatosis: Report of a Case with a Novel ANTXR2 Gene Mutation
Patient: Female, 2-year-old Final Diagnosis: Juvenile hyaline fibromatosis Symptoms: Multiple painless soft tissue masses affecting the ears • forehead • scalp Medication: — Clinical Procedure: Excision biopsy • surgery removal Specialty: Pediatrics and Neonatology • Surgery OBJECTIVE: Rare disease...
Autores principales: | Choochuen, Pongsakorn, Laochareonsuk, Wison, Tanaanantarak, Pattama, Kanjanapradit, Kanet, Sangkhathat, Surasak |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9245060/ https://www.ncbi.nlm.nih.gov/pubmed/35752930 http://dx.doi.org/10.12659/AJCR.935921 |
Ejemplares similares
-
Prevalence of Pathogenic Germline Mutations in 13 Hereditary Cancer-Related Genes in Breast Cancer Patients in Narathiwat Province, Thailand
por: Sukpan, Panupong, et al.
Publicado: (2023) -
Multiple Scalp Tumors in Juvenile Hyaline Fibromatosis with Antxr-2 Mutation in a Family
por: Mendiratta, Vibhu, et al.
Publicado: (2021) -
A Case of Hyaline Fibromatosis Syndrome with a New Variant of Genetic Mutation in ANTXR2 Gene
por: Park, Chan Seong, et al.
Publicado: (2019) -
Exome Sequencing Reveals Novel Germline Variants in Breast Cancer Patients in the Southernmost Region of Thailand
por: Sukpan, Panupong, et al.
Publicado: (2023) -
Juvenile Hyaline Fibromatosis
por: Park, Kyung Tae, et al.
Publicado: (2010)